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Treatment of central serous chorioretinopathy with topical NSAIDs
PURPOSE: Central serous chorioretinopathy (CSCR) is a common retinopathy that is often observed until resolution. The purpose of this study is to evaluate the effects of topical nonsteroidal anti-inflammatory drugs (NSAIDs) on timing of CSCR recovery. METHODS: An IRB-approved retrospective review wa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6699520/ https://www.ncbi.nlm.nih.gov/pubmed/31616132 http://dx.doi.org/10.2147/OPTH.S202047 |
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author | Bahadorani, Sepehr Maclean, Kyle Wannamaker, Kendall Chu, Edward Rickie Gresores, Nathan Sohn, Jeong-Hyeon Diaz-Rohena, Roberto Singer, Michael A |
author_facet | Bahadorani, Sepehr Maclean, Kyle Wannamaker, Kendall Chu, Edward Rickie Gresores, Nathan Sohn, Jeong-Hyeon Diaz-Rohena, Roberto Singer, Michael A |
author_sort | Bahadorani, Sepehr |
collection | PubMed |
description | PURPOSE: Central serous chorioretinopathy (CSCR) is a common retinopathy that is often observed until resolution. The purpose of this study is to evaluate the effects of topical nonsteroidal anti-inflammatory drugs (NSAIDs) on timing of CSCR recovery. METHODS: An IRB-approved retrospective review was conducted on patients that had been diagnosed with a new-onset, symptomatic case of CSCR. Patients were either observed only (13 untreated eyes) or treated with topical bromfenac or nepafenac (14 eyes) over an average of about a 4–5 week follow-up period. RESULTS: There was no statistical significance between central macular thickness (CMT) and visual acuity of treatment and control groups at the initial presentation. However, at the follow-up visit, CMT reductions in the treatment group were significantly higher than in the control group (p<0.006). CONCLUSION: Use of topical NSAIDs in the treatment of acute CSCR leads to a faster rate of reduction in the subretinal fluid volume over a follow-up period of a few weeks. |
format | Online Article Text |
id | pubmed-6699520 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-66995202019-10-15 Treatment of central serous chorioretinopathy with topical NSAIDs Bahadorani, Sepehr Maclean, Kyle Wannamaker, Kendall Chu, Edward Rickie Gresores, Nathan Sohn, Jeong-Hyeon Diaz-Rohena, Roberto Singer, Michael A Clin Ophthalmol Original Research PURPOSE: Central serous chorioretinopathy (CSCR) is a common retinopathy that is often observed until resolution. The purpose of this study is to evaluate the effects of topical nonsteroidal anti-inflammatory drugs (NSAIDs) on timing of CSCR recovery. METHODS: An IRB-approved retrospective review was conducted on patients that had been diagnosed with a new-onset, symptomatic case of CSCR. Patients were either observed only (13 untreated eyes) or treated with topical bromfenac or nepafenac (14 eyes) over an average of about a 4–5 week follow-up period. RESULTS: There was no statistical significance between central macular thickness (CMT) and visual acuity of treatment and control groups at the initial presentation. However, at the follow-up visit, CMT reductions in the treatment group were significantly higher than in the control group (p<0.006). CONCLUSION: Use of topical NSAIDs in the treatment of acute CSCR leads to a faster rate of reduction in the subretinal fluid volume over a follow-up period of a few weeks. Dove 2019-08-15 /pmc/articles/PMC6699520/ /pubmed/31616132 http://dx.doi.org/10.2147/OPTH.S202047 Text en © 2019 Bahadorani et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Bahadorani, Sepehr Maclean, Kyle Wannamaker, Kendall Chu, Edward Rickie Gresores, Nathan Sohn, Jeong-Hyeon Diaz-Rohena, Roberto Singer, Michael A Treatment of central serous chorioretinopathy with topical NSAIDs |
title | Treatment of central serous chorioretinopathy with topical NSAIDs |
title_full | Treatment of central serous chorioretinopathy with topical NSAIDs |
title_fullStr | Treatment of central serous chorioretinopathy with topical NSAIDs |
title_full_unstemmed | Treatment of central serous chorioretinopathy with topical NSAIDs |
title_short | Treatment of central serous chorioretinopathy with topical NSAIDs |
title_sort | treatment of central serous chorioretinopathy with topical nsaids |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6699520/ https://www.ncbi.nlm.nih.gov/pubmed/31616132 http://dx.doi.org/10.2147/OPTH.S202047 |
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